A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children's Oncology Group study. [electronic resource]
Producer: 20190507Description: e0208936 p. digitalISSN:- 1932-6203
- Anaplasia -- genetics
- Carcinogenesis -- genetics
- DNA Methylation -- genetics
- Female
- Germ-Line Mutation -- genetics
- HEK293 Cells
- Humans
- Infant
- Infant, Newborn
- Kidney -- growth & development
- Kidney Neoplasms -- genetics
- Loss of Function Mutation -- genetics
- Male
- Risk Factors
- Tripartite Motif-Containing Protein 28 -- genetics
- Wilms Tumor -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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